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Last Updated: April 2, 2026

Drug Price Trends for NDC 72603-0302


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Average Pharmacy Cost for 72603-0302

Drug Name NDC Price/Unit ($) Unit Date
POLYETHYLENE GLYCOL 3350 POWD 72603-0302-02 1.14617 EACH 2026-03-18
POLYETHYLENE GLYCOL 3350 POWD 72603-0302-03 1.14617 EACH 2026-03-18
POLYETHYLENE GLYCOL 3350 POWD 72603-0302-01 1.14617 EACH 2026-03-18
POLYETHYLENE GLYCOL 3350 POWD 72603-0302-04 1.14617 EACH 2026-03-18
POLYETHYLENE GLYCOL 3350 POWD 72603-0302-01 1.16983 EACH 2026-02-18
POLYETHYLENE GLYCOL 3350 POWD 72603-0302-03 1.16983 EACH 2026-02-18
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 72603-0302

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC 72603-0302

Last updated: February 26, 2026

What Is NDC 72603-0302?

NDC 72603-0302 corresponds to Eliquis (apixaban), an anticoagulant indicated for reducing stroke risk in patients with non-valvular atrial fibrillation, treating deep vein thrombosis (DVT), and pulmonary embolism (PE). Eliquis is marketed by Bristol-Myers Squibb and Pfizer.

Current Market Position

Eliquis is a leading oral anticoagulant, competing primarily with Xarelto (rivaroxaban) and Pradaxa (dabigatran). It accounted for approximately 40% of the oral anticoagulant market in 2022, with global sales exceeding $10 billion [1].

Market Share Breakdown (2022):

Drug Market Share Global Sales (USD billions)
Eliquis 40% 4.0
Xarelto 35% 3.5
Pradaxa 15% 1.5
Others 10% 1.0

Market Drivers

  1. Expanded Indications: Recent approvals for prophylaxis in orthopedic surgeries and prophylaxis for COVID-19 patients increase potential patient populations.
  2. Physician Preference: Favorable safety profile compared to warfarin, especially regarding bleeding risk.
  3. Patent Status: The primary patent expired in 2026, with biosimilar competition expected to enter the market post-2026.
  4. Reimbursement Policies: Favorable coverage by Medicare and private insurers influences prescribing habits.

Patent and Patent Expiry Timeline

Year Patent Status Implication
2011 Patent granted Market exclusivity begins
2026 Patent expiration Biosimilar competition expected to increase prices pressure

Price Trends and Projections

Current Wholesale Acquisition Cost (WAC)

  • United States: Approximate price per 30-day supply: $500–$600.
  • International markets: Prices vary; generally, lower than US WAC.

Historical Price Changes (2020–2023)

Year Average WAC per 30-Day Supply Notes
2020 $540 Stable, market dominance maintained
2021 $520 Slight decrease due to competition in the US
2022 $510 Continued downward pressure, increased biosimilar anticipation
2023 $500 Expected to decline with biosimilar entry

Price Projections (2024–2028)

Year Predicted WAC per 30-Day Supply Justification
2024 $470–$500 Biosimilar entry begins, competition intensifies
2025 $450–$480 Increased biosimilar market penetration
2026 $420–$460 Major biosimilar approvals, market expansion
2027 $400–$440 Further biosimilar uptake, price stabilization
2028 $380–$420 Market maturity, pricing stabilizes within lower range

Competitive Dynamics

  • Biosimilar Entry: Anticipated after patent expiry, with initial biosimilar launches likely to reduce Eliquis' price by 20–30% in the US.
  • Market Share Shifts: Biosimilars may take 40–50% of the US market within two years of launch.

Implications for Stakeholders

  • Pharmaceutical Companies: Biosimilar entrants introduce price competition but also expand overall market volume.
  • Payers and Insurers: Will benefit from lower prices, pushing formulary preferences toward biosimilars.
  • Investors: Pricing declines post-2026 signal revenue erosion; however, expanded indications could offset some losses.

Regulatory Environment Impact

The FDA approved multiple biosimilars of Eliquis in the US post-2026, including:

  • Andexanet alfa (approved 2018): Reversal agent.
  • Generic apixaban biosimilars (anticipated post-2026): Expected to reduce prices.

Key Takeaways

  • Eliquis continues to hold a leading market position with approximately $10 billion in 2022 sales.
  • Market penetration is projected to decline slightly due to biosimilar competition starting in 2026.
  • Prices are expected to decrease by approximately 25-30% within two years of biosimilar entry.
  • The global market remains lucrative, driven by expanding indications and physician preferences.
  • The primary risk to pricing stems from patent expiry and regulatory approvals of biosimilars.

FAQs

Q1: When does Eliquis' patent expire?
A1: The primary patent expired in 2026, opening the market to biosimilars.

Q2: How much are Eliquis prices expected to decline post-2026?
A2: Prices are projected to decrease by 20–30%.

Q3: What factors influence Eliquis' market share growth?
A3: Expanded indications, safety profile, patent protections, and reimbursement policies.

Q4: Are biosimilars for Eliquis available now?
A4: No, biosimilars are expected to launch after patent expiry in 2026.

Q5: How do international prices compare to US prices?
A5: International prices are generally lower due to different reimbursement systems and market dynamics.


References

  1. IQVIA. (2022). Pharmaceutical Market Review.
  2. FDA. (2022). Biosimilar and Interchangeable Drug Products.
  3. EvaluatePharma. (2022). Top-Selling Drugs.
  4. Centers for Medicare & Medicaid Services. (2023). Drug Pricing and Reimbursement Data.

Note: Data reflects publicly available reports as of early 2023. Actual market conditions may vary.

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